FDA Registration
Active
🇺🇸 United States
dBest MultiDrug Screen Test Kit
Reg #: 3025672
·
FEI: 1000126037
·
Expires 2025
Products
5
Proprietary Names
1
Establishment Types
1
Classifications
5
Registration Details
- Registration Name
- AMERITEK USA, INC.
- Registration Number
- 3025672
- FEI Number
- 1000126037
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- 125 130th St SE Ste 200
- City
- EVERETT
- State
- WA
- ZIP
- 98208
- Country
- US
Regulatory Submissions
- 510(k) Number
- K990681
Owner / Operator
- Firm Name
- AMERITEK USA, INC.
- Operator Number
- 9002732
- Address
- 125 130 TH STREET SE, --
- City
- Everett
- State
- WA
- Postal Code
- 98208
- Country
- US
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Enzyme Immunoassay, Amphetamine | DKZ | Class 2 | Clinical Toxicology | No | 2008-05-11 |
| Gas Chromatography, Methamphetamine | LAF | Class 2 | Clinical Toxicology | No | 2008-05-11 |
| Enzyme Immunoassay, Opiates | DJG | Class 2 | Clinical Toxicology | No | 2008-05-11 |
| Enzyme Immunoassay, Cocaine And Cocaine Metabolites | DIO | Class 2 | Clinical Toxicology | No | 2008-05-11 |
| Enzyme Immunoassay, Cannabinoids | LDJ | Class 2 | Clinical Toxicology | No | 2008-05-11 |
Proprietary Names
dBest MultiDrug Screen Test Kit
Establishment Types
Manufacture Medical Device